Akhmanova Anna, Stehbens Samantha J, Yap Alpha S
Department of Cell Biology, Erasmus Medical Center, Rotterdam, The Netherlands.
Traffic. 2009 Mar;10(3):268-74. doi: 10.1111/j.1600-0854.2008.00869.x. Epub 2009 Jan 17.
Cross-talk between microtubule networks and sites of cell-matrix and cell-cell adhesion has profound impact on these structures and is essential for proper cell organization, polarization and motility. Components of adhesion sites can interact directly with microtubules or with proteins that specifically associate with microtubule plus ends and minus ends and in this way capture, stabilize or destabilize microtubules. In their turn, microtubules can serve as routes for delivery of structural and regulatory factors that control adhesion site turnover. In addition, the microtubule lattice or growing microtubule plus ends can serve as diffusional sinks that accumulate and scaffold regulatory molecules, thereby affecting their activity in the vicinity of adhesions. Combination of these mechanisms underlies the functional co-operation between microtubules and adhesion sites and defines their dynamic behavior.
微管网络与细胞-基质及细胞-细胞黏附位点之间的相互作用对这些结构有着深远影响,对于细胞的正常组织、极化和运动至关重要。黏附位点的组分可直接与微管相互作用,或与特异性结合微管正端和负端的蛋白质相互作用,从而以这种方式捕获、稳定或破坏微管。反过来,微管可作为控制黏附位点更新的结构和调节因子的输送途径。此外,微管晶格或生长中的微管正端可作为扩散汇,积累并支撑调节分子,从而影响它们在黏附附近的活性。这些机制的结合构成了微管与黏附位点之间功能协作的基础,并定义了它们的动态行为。